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Low-dose aspirin does not interfere with the blood pressure-lowering effects of antihypertensive therapy
Alberto Zanchetti1, Lennart Hansson, Gastone Leonetti
1Centro di Fisiologia Clinica e Ipertensione, Università di Milano, Ospedale Maggiore and Istituto Auxologico Italiano, Milano, Italy. zanchett@mailserver.unimi.it
Insights
Low-dose aspirin (ASA) does not affect blood pressure control or kidney function in hypertensive patients, even when combined with angiotensin-converting enzyme (ACE) inhibitors. Cardiovascular benefits of aspirin remain consistent across these treatment groups.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Nephrology
Background:
- Aspirin (ASA) has been suspected of interfering with antihypertensive medications.
- Concerns exist regarding potential attenuation of angiotensin-converting enzyme (ACE) inhibitor benefits by ASA in heart failure patients.
Purpose of the Study:
- To reanalyze data from the Hypertension Optimal Treatment (HOT) Study to assess the effects of low-dose aspirin on blood pressure and renal function in hypertensive patients.
- To investigate potential interactions between aspirin, antihypertensive agents, and ACE inhibitors.
Main Methods:
- Reanalysis of data from 18,790 hypertensive patients in the HOT Study, randomized to aspirin (75 mg daily) or placebo for 3.8 years.
- Examination of effects on systolic blood pressure (SBP), diastolic blood pressure (DBP), serum creatinine, and estimated creatinine clearance.
- Comparison of cardiovascular event rates and renal dysfunction incidence between aspirin and placebo groups, including subgroups receiving ACE inhibitors.
Main Results:
- Systolic and diastolic blood pressure control was similar between aspirin-treated and placebo groups.
- Antihypertensive therapies were comparable in both groups.
- Changes in renal function markers (serum creatinine, creatinine clearance) and incidence of renal dysfunction were similar.
- Cardiovascular benefits of aspirin were consistent in patients receiving or not receiving ACE inhibitors.
Conclusions:
- Long-term, low-dose aspirin does not interfere with blood pressure lowering by antihypertensive agents, including ACE inhibitors.
- No negative interaction was observed between ACE inhibition and the cardiovascular benefits of low-dose aspirin.
- Findings do not apply to higher aspirin doses or patients with congestive heart failure.
Background:
It has been reported that aspirin (ASA) may interfere with the blood pressure (BP)-lowering effect of various antihypertensive agents and attenuate the beneficial effects of angiotensin-converting enzyme (ACE) inhibitors in patients with congestive heart failure.
Methods And Results:
Data from the Hypertension Optimal Treatment (HOT) Study, in which 18 790 intensively treated hypertensive patients were randomized to either ASA 75 mg daily or placebo for 3.8 years (with a 15% reduction in cardiovascular events and a 36% reduction in myocardial infarction in ASA-treated patients), were reanalysed for the whole group of patients and for various subgroups with particular attention to the possible effects of ASA on BP and renal function. In ASA-treated and placebo-treated patients: (1) systolic blood pressure (SBP) and diastolic blood pressure (DBP) values achieved with antihypertensive treatment were superimposable, with clinically irrelevant differences; (2) these superimposable SBP and DBP were achieved with antihypertensive therapies, that were quantitatively and qualitatively similar, and (3) changes in serum creatinine and in estimated creatinine clearance and the number of patients developing renal dysfunction were also similar. Furthermore, the cardiovascular benefits of ASA were of the same magnitude in hypertensive patients receiving or not receiving ACE-inhibitors.
Conclusions:
Even long-term, low-dose ASA does not interfere with the BP-lowering effect of antihypertensive agents, including combinations with ACE inhibitors, or with renal function. No negative interaction occurs between ACE inhibition and the cardiovascular benefits of small dose of ASA. Our conclusions cannot be extended to larger doses of ASA, or to patients with congestive heart failure.
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